ZÁZNAM | Proběhlo Čt, 18.4.2024
Na tomto webináři se dozvíte, co je to IVDR a jaké jsou časové lhůty, jaké jsou požadavky na interní testy a jaké jsou další kroky pro vaši laboratoř.Přejít na webinář
Making sense of IVDR for LC-MS
SCIEX: Making sense of IVDR for LC-MS
In Vitro Diagnostic Regulation (IVDR) is the European Union’s new set of rules aimed at improving the quality, safety and reliability of IVDs. The new regulation is impacting the in vitro diagnostic landscape, affecting laboratories using their own “Laboratory Developed Tests” (LDTs) and those compliant with certain accreditation e.g. standard EN ISO 15189.
In this webinar you will learn:
- What is IVDR and what are the timelines
- What are the requirements for in-house tests (LDTs)
- What are the next steps for your lab
Presenter: Fabian Reijn (Diagnotix)
Presenter: Magali Wolff (Tecan)
